Sandra Monfort

1.2k total citations
41 papers, 530 citations indexed

About

Sandra Monfort is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sandra Monfort has authored 41 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 20 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sandra Monfort's work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Prenatal Screening and Diagnostics (9 papers). Sandra Monfort is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Prenatal Screening and Diagnostics (9 papers). Sandra Monfort collaborates with scholars based in Spain, Netherlands and Lithuania. Sandra Monfort's co-authors include Francisco Martı́nez, Carmen Orellana, Silvestre Oltra, Mónica Rosello, Sonia Mayo, Alfonso Caro‐Llopis, Jeremy Howard, Budhan S. Pukazhenthi, Timothy C. Roth and D. E. Wildt and has published in prestigious journals such as Scientific Reports, BioMed Research International and Journal of Medical Genetics.

In The Last Decade

Sandra Monfort

38 papers receiving 519 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sandra Monfort Spain 13 364 264 94 50 49 41 530
B Delobel France 11 313 0.9× 170 0.6× 117 1.2× 85 1.7× 60 1.2× 18 451
Azzedine Aboura France 17 525 1.4× 311 1.2× 258 2.7× 110 2.2× 61 1.2× 40 767
Vikram Jaswaney United States 7 424 1.2× 245 0.9× 154 1.6× 51 1.0× 60 1.2× 12 489
Stefanie Eggers Australia 15 450 1.2× 466 1.8× 47 0.5× 21 0.4× 100 2.0× 25 728
Alexandra M. Lopes Portugal 15 424 1.2× 392 1.5× 28 0.3× 80 1.6× 150 3.1× 36 685
Céline Dupont France 15 328 0.9× 213 0.8× 123 1.3× 88 1.8× 9 0.2× 38 645
D Robinson United Kingdom 10 410 1.1× 269 1.0× 95 1.0× 105 2.1× 32 0.7× 14 534
Lisskulla Sylvén Sweden 10 455 1.3× 231 0.9× 53 0.6× 36 0.7× 61 1.2× 12 653
Joo Wook Ahn United Kingdom 13 424 1.2× 232 0.9× 159 1.7× 72 1.4× 4 0.1× 29 605
Françoise Devillard France 11 247 0.7× 152 0.6× 142 1.5× 78 1.6× 148 3.0× 27 431

Countries citing papers authored by Sandra Monfort

Since Specialization
Citations

This map shows the geographic impact of Sandra Monfort's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sandra Monfort with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Monfort more than expected).

Fields of papers citing papers by Sandra Monfort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra Monfort. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sandra Monfort. The network helps show where Sandra Monfort may publish in the future.

Co-authorship network of co-authors of Sandra Monfort

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Monfort. A scholar is included among the top collaborators of Sandra Monfort based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sandra Monfort. Sandra Monfort is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Caro‐Llopis, Alfonso, Mónica Rosello, Silvestre Oltra, et al.. (2025). Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study. Amyloid. 32(4). 324–334.
2.
3.
Caro‐Llopis, Alfonso, et al.. (2022). Extending the Phenotype Related to SCN1A Gene: Arthrogryposis, Movement Disorders, and Malformations of Cortical Development. Journal of Child Neurology. 37(5). 340–350. 2 indexed citations
4.
Tomás‐Vila, Miguel, Juan J. Vílchez, Inmaculada Azorı́n, et al.. (2021). Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene. Clinical Genetics. 101(2). 233–241. 9 indexed citations
5.
Caro‐Llopis, Alfonso, et al.. (2021). Extending the clinical phenotype of SPTAN1: From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability. American Journal of Medical Genetics Part A. 188(1). 147–159. 6 indexed citations
6.
Monfort, Sandra, Carmen Orellana, Silvestre Oltra, et al.. (2021). Prevalence of pathogenic copy number variants among children conceived by donor oocyte. Scientific Reports. 11(1). 6752–6752. 2 indexed citations
7.
Rosello, Mónica, Alfonso Caro‐Llopis, Carmen Orellana, et al.. (2020). Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing. Pediatric Research. 90(2). 284–288. 26 indexed citations
8.
Preikšaitienė, Eglė, Alfonso Caro‐Llopis, Silvestre Oltra, et al.. (2015). A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome. American Journal of Medical Genetics Part A. 167(6). 1342–1348. 7 indexed citations
9.
Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2015). In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients. BioMed Research International. 2015. 1–8. 3 indexed citations
10.
Martı́nez, Francisco, Purificación Marín Reina, Antonio Pérez Aytés, et al.. (2015). Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes. Pediatric Research. 78(5). 533–539. 28 indexed citations
11.
López-Carrasco, Amparo, Sandra Monfort, Mónica Rosello, et al.. (2013). Localización cromosómica de duplicaciones submicroscópicas en pacientes con trastornos del neurodesarrollo para identificar casos con alto riesgo de recurrencia familiar. Medicina Clínica. 142(12). 531–537. 3 indexed citations
12.
Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2011). De novo Interstitial Triplication of <i>MECP2</i> in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation. Cytogenetic and Genome Research. 135(2). 93–101. 19 indexed citations
13.
Monfort, Sandra, Silvestre Oltra, Mónica Rosello, et al.. (2011). Partial Duplication of 18q Including a Distal Critical Region for Edwards Syndrome in a Patient with Normal Phenotype and Oligoasthenospermia: Case Report. Cytogenetic and Genome Research. 133(1). 78–83. 7 indexed citations
14.
Rosello, Mónica, et al.. (2009). Rare chromosomal complement of trisomy 21 in a boy conceived by IVF and cryopreservation. Reproductive BioMedicine Online. 19(3). 415–417. 2 indexed citations
15.
Rosello, Mónica, et al.. (2009). Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion. Cytogenetic and Genome Research. 125(2). 103–108. 11 indexed citations
16.
Rosello, Mónica, Sandra Monfort, Silvestre Oltra, et al.. (2009). Prenatal study of common submicroscopic “genomic disorders” using MLPA with subtelomeric/microdeletion syndrome probe mixes, among gestations with ultrasound abnormalities in the first trimester. European Journal of Medical Genetics. 53(2). 76–79. 5 indexed citations
17.
Rosello, Mónica, Sandra Monfort, Carmen Orellana, et al.. (2007). Deleción subtelomérica 9qter: definición del síndrome y origen parental en 2 pacientes. Medicina Clínica. 128(11). 419–421. 4 indexed citations
18.
Martı́nez, Francisco, Ana M. León, Sandra Monfort, et al.. (2006). Robust, Easy, and Dose-Sensitive Methylation Test for the Diagnosis of Prader–Willi and Angelman Syndromes. Genetic Testing. 10(3). 174–177. 8 indexed citations
19.
Orellana, Carmen, Lourdes Badı́a, Francisco Martı́nez, et al.. (2006). Recombinant X chromosome in a prenatal diagnosis. Cytogenetic and Genome Research. 112(3-4). 337–340. 3 indexed citations
20.
Wildt, D. E., Budhan S. Pukazhenthi, Janine L. Brown, et al.. (1995). Spermatology for understanding, managing and conserving rare species. Reproduction Fertility and Development. 7(4). 811–824. 56 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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